Kesari A - Search Results

1

Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B.

Nagaraju K, Rawat R, Veszelovszky E, Thapliyal R, Kesari A, Sparks S, Raben N, Plotz P, Hoffman EP. Nagaraju K, et al. Among authors: kesari a. Am J Pathol. 2008 Mar;172(3):774-85. doi: 10.2353/ajpath.2008.070327. Epub 2008 Feb 14. Am J Pathol. 2008. PMID: 18276788 Free PMC article.

2

Dysferlin deficiency shows compensatory induction of Rab27A/Slp2a that may contribute to inflammatory onset.

Kesari A, Fukuda M, Knoblach S, Bashir R, Nader GA, Rao D, Nagaraju K, Hoffman EP. Kesari A, et al. Am J Pathol. 2008 Nov;173(5):1476-87. doi: 10.2353/ajpath.2008.080098. Epub 2008 Oct 2. Am J Pathol. 2008. PMID: 18832576 Free PMC article.

3

Non-invasive optical imaging of muscle pathology in mdx mice using cathepsin caged near-infrared imaging.

Baudy AR, Sali A, Jordan S, Kesari A, Johnston HK, Hoffman EP, Nagaraju K. Baudy AR, et al. Among authors: kesari a. Mol Imaging Biol. 2011 Jun;13(3):462-470. doi: 10.1007/s11307-010-0376-z. Mol Imaging Biol. 2011. PMID: 20661652 Free PMC article.

4

Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy.

Dadgar S, Wang Z, Johnston H, Kesari A, Nagaraju K, Chen YW, Hill DA, Partridge TA, Giri M, Freishtat RJ, Nazarian J, Xuan J, Wang Y, Hoffman EP. Dadgar S, et al. Among authors: kesari a. J Cell Biol. 2014 Oct 13;207(1):139-58. doi: 10.1083/jcb.201402079. J Cell Biol. 2014. PMID: 25313409 Free PMC article.

5

Somatic mosaicism for Duchenne dystrophy: evidence for genetic normalization mitigating muscle symptoms.

Kesari A, Neel R, Wagoner L, Harmon B, Spurney C, Hoffman EP. Kesari A, et al. Am J Med Genet A. 2009 Jul;149A(7):1499-503. doi: 10.1002/ajmg.a.32891. Am J Med Genet A. 2009. PMID: 19530190 Free PMC article.

6

Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule.

Kesari A, Pirra LN, Bremadesam L, McIntyre O, Gordon E, Dubrovsky AL, Viswanathan V, Hoffman EP. Kesari A, et al. Hum Mutat. 2008 May;29(5):728-37. doi: 10.1002/humu.20722. Hum Mutat. 2008. PMID: 18348289

7

Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spine.

O'Grady GL, Best HA, Oates EC, Kaur S, Charlton A, Brammah S, Punetha J, Kesari A, North KN, Ilkovski B, Hoffman EP, Clarke NF. O'Grady GL, et al. Among authors: kesari a. Eur J Hum Genet. 2015 Jun;23(6):883-6. doi: 10.1038/ejhg.2014.169. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182138 Free PMC article.

8

Somatic mosaicism due to a reversion variant causing hemi-atrophy: a novel variant of dystrophinopathy.

Punetha J, Mansoor S, Bertorini TE, Kesari A, Brown KJ, Hoffman EP. Punetha J, et al. Among authors: kesari a. Eur J Hum Genet. 2016 Oct;24(10):1511-4. doi: 10.1038/ejhg.2016.22. Epub 2016 Mar 9. Eur J Hum Genet. 2016. PMID: 26956251 Free PMC article.

9

Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.

Punetha J, Kesari A, Uapinyoying P, Giri M, Clarke NF, Waddell LB, North KN, Ghaoui R, O'Grady GL, Oates EC, Sandaradura SA, Bönnemann CG, Donkervoort S, Plotz PH, Smith EC, Tesi-Rocha C, Bertorini TE, Tarnopolsky MA, Reitter B, Hausmanowa-Petrusewicz I, Hoffman EP. Punetha J, et al. Among authors: kesari a. J Neuromuscul Dis. 2016 May 27;3(2):209-225. doi: 10.3233/JND-160151. J Neuromuscul Dis. 2016. PMID: 27854218

10

PCB congener specific oxidative stress response by microarray analysis using human liver cell line.

De S, Ghosh S, Chatterjee R, Chen YQ, Moses L, Kesari A, Hoffman EP, Dutta SK. De S, et al. Among authors: kesari a. Environ Int. 2010 Nov;36(8):907-17. doi: 10.1016/j.envint.2010.05.011. Epub 2010 Jul 17. Environ Int. 2010. PMID: 20638727 Free PMC article.

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